A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559166



Internal ID20932237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:98629274..99014615hg38UCSC Ensembl
chr4:99550425..99935766hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38385342
hg19385342
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18265486
Samples
Known GenesEIF4E, METAP1, MIR3684, TSPAN5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559166
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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